DK33792D0 - Krystalform af aminoalkylfuranderivat - Google Patents

Krystalform af aminoalkylfuranderivat

Info

Publication number
DK33792D0
DK33792D0 DK92337A DK33792A DK33792D0 DK 33792 D0 DK33792 D0 DK 33792D0 DK 92337 A DK92337 A DK 92337A DK 33792 A DK33792 A DK 33792A DK 33792 D0 DK33792 D0 DK 33792D0
Authority
DK
Denmark
Prior art keywords
aminoal
crystal form
reference derivative
cool
cool reference
Prior art date
Application number
DK92337A
Other languages
English (en)
Other versions
DK167923B1 (da
DK33792A (da
Inventor
Derek Leslie Crookes
Original Assignee
Glaxo Group Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=10516407&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=DK33792(D0) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Glaxo Group Ltd filed Critical Glaxo Group Ltd
Publication of DK33792A publication Critical patent/DK33792A/da
Publication of DK33792D0 publication Critical patent/DK33792D0/da
Application granted granted Critical
Publication of DK167923B1 publication Critical patent/DK167923B1/da

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D307/52—Radicals substituted by nitrogen atoms not forming part of a nitro radical
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Furan Compounds (AREA)
DK033792A 1980-10-01 1992-03-12 Ranitidinhydrochlorid i form 2 og anvendelsen deraf ved fremstilling af et farmaceutisk praeparat DK167923B1 (da)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB8031634 1980-10-01
GB8031634 1980-10-01

Publications (3)

Publication Number Publication Date
DK33792A DK33792A (da) 1992-03-12
DK33792D0 true DK33792D0 (da) 1992-03-12
DK167923B1 DK167923B1 (da) 1994-01-03

Family

ID=10516407

Family Applications (2)

Application Number Title Priority Date Filing Date
DK436281A DK167794B1 (da) 1980-10-01 1981-10-01 Fremgangsmaade til fremstilling af en krystalform af ranitidinhydrochlorid
DK033792A DK167923B1 (da) 1980-10-01 1992-03-12 Ranitidinhydrochlorid i form 2 og anvendelsen deraf ved fremstilling af et farmaceutisk praeparat

Family Applications Before (1)

Application Number Title Priority Date Filing Date
DK436281A DK167794B1 (da) 1980-10-01 1981-10-01 Fremgangsmaade til fremstilling af en krystalform af ranitidinhydrochlorid

Country Status (29)

Country Link
US (2) US4521431A (da)
JP (1) JPS5791983A (da)
KR (1) KR870001431B1 (da)
AT (1) AT389696B (da)
AU (1) AU549119B2 (da)
BE (1) BE890574A (da)
CA (1) CA1202638A (da)
CH (1) CH652122A5 (da)
CZ (1) CZ280885B6 (da)
DE (1) DE3139134A1 (da)
DK (2) DK167794B1 (da)
ES (1) ES8301954A1 (da)
FR (1) FR2491067A1 (da)
GR (1) GR72499B (da)
HK (1) HK97985A (da)
IE (1) IE51604B1 (da)
IL (1) IL63968A (da)
IT (1) IT1143237B (da)
KE (1) KE3549A (da)
LU (1) LU83661A1 (da)
MY (1) MY8500747A (da)
NL (1) NL8104482A (da)
NZ (1) NZ198522A (da)
PH (2) PH19489A (da)
PT (1) PT73744B (da)
SE (1) SE453500B (da)
SK (1) SK277922B6 (da)
ZA (1) ZA816809B (da)
ZW (1) ZW24481A1 (da)

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SE8704436D0 (sv) * 1987-11-13 1987-11-13 Pm Konsult Handelsbolag Anvendning av antisekretoriska substanser for nya indikationer
IL90245A (en) * 1988-05-11 1994-04-12 Glaxo Group Ltd Resin adsorption containing ranitidine together with synthetic resin replaces cations, its preparation and pharmaceutical preparations containing it
GB8904182D0 (en) * 1989-02-23 1989-04-05 Glaxo Canada Pharmaceutical compositions
US5169864A (en) * 1991-11-15 1992-12-08 Baxter International Inc. Unbuffered premixed ranitidine formulation
US5338871A (en) * 1991-12-20 1994-08-16 Torcan Chemical Ltd. Preparation of form 1 ranitidine hydrochloride
CN1048984C (zh) * 1991-12-20 2000-02-02 多坎化学有限公司 晶形1呋喃硝胺氢氯化物的制备
PL184611B1 (pl) * 1993-03-12 2002-11-29 Upjohn Co Krystaliczny ceftiofur w postaci wolnego kwasu sposób jego wytwarzania oraz kompozycja farmaceutyczna zawierająca krystaliczny ceftiofur w postaci wolnego kwasu
DE4341310A1 (de) * 1993-12-03 1995-06-08 Hexal Pharma Gmbh Tablette oder Kapsel mit einem Gehalt an stabilem Ranitidinhydrochlorid Form 1
US5407687A (en) * 1994-02-22 1995-04-18 Glaxo Inc. Ranitidine solid dosage form
CA2120874E (en) * 1994-04-08 2002-01-08 Keshava Murthy Form of form 1 ranitidine
US5670671A (en) * 1994-04-08 1997-09-23 Brantford Chemicals Inc. Process for the production of an improved form of form 1 ranitidine
PT755393E (pt) 1994-04-15 2002-04-29 Upjohn Co Novas formas cristalinas de 1-¬5-metanossulfonamidoimdolil-2-carbonil|-4-¬3-(1-metiletilamino)-2-piridinil|piperazina
IN181699B (da) * 1994-05-13 1998-09-05 Ranbaxy Lab Ltd
IN181698B (da) * 1994-05-13 1998-09-05 Ranbaxy Lab Ltd
NZ272054A (en) * 1994-05-13 1996-05-28 Ranbaxy Lab Ltd Process for producing form 1 ranitidine hydrochloride
WO1995031437A1 (en) * 1994-05-18 1995-11-23 Hoechst Marrion Roussel, Inc. Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudormophs thereof
US20030045722A1 (en) * 1994-05-18 2003-03-06 Henton Daniel R. Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof
DE69504156T2 (de) 1994-06-24 1998-12-24 Ranbaxy Laboratories, Ltd., New Delhi Verfahren zur Herstellung von Ranitidinhydrochlorid in der Kristallform 1
PL320190A1 (en) * 1994-11-18 1997-09-15 Upjohn Co Novel, physically stable form of fuoroquinolone
US5538737A (en) * 1994-11-30 1996-07-23 Applied Analytical Industries, Inc. Oral compositions of H2 -antagonists
US5663381A (en) * 1995-04-21 1997-09-02 Hexal Pharmaceuticals, Inc. Process for preparing form 1 ranitidine hydrochloride
US5686588A (en) * 1995-08-16 1997-11-11 Yoo; Seo Hong Amine acid salt compounds and process for the production thereof
WO1997035853A1 (en) * 1996-03-25 1997-10-02 Hoechst Marion Roussel, Inc. Process for the preparation of form 1 ranitidine hydrochloride
DE59801792D1 (de) * 1997-08-08 2001-11-22 Aventis Pharma Gmbh Kristallform von N-(4-Trifluormethylphenyl)-5-methylisoxazol-4-carbonsäureamid
US6287693B1 (en) 1998-02-25 2001-09-11 John Claude Savoir Stable shaped particles of crystalline organic compounds
IT1317858B1 (it) 2000-02-29 2003-07-15 Pharmexcel S R L Allomorfo del cloridrato dell'isomero z di derivato dialchilamminofurano, procedimento per la sua produzione e composizione
GB2357762B (en) * 2000-03-13 2002-01-30 Lundbeck & Co As H Crystalline base of citalopram
US20020183553A1 (en) * 2000-10-19 2002-12-05 Ben-Zion Dolitzky Crystalline venlafaxine base and novel polymorphs of venlafaxine hydrochloride, processes for preparing thereof
US6569887B2 (en) * 2001-08-24 2003-05-27 Dov Pharmaceuticals Inc. (−)-1-(3,4-Dichlorophenyl)-3-azabicyclo[3.1.0]hexane, compositions thereof, and uses as a dopamine-reuptake
US20060173064A1 (en) * 2001-08-24 2006-08-03 Lippa Arnold S (-)-1-(3,4-Dichlorophenyl)-3-azabi cyclo[3.1.0]hexane, compositions thereof, and uses for treating alcohol-related disorders
US7235655B2 (en) * 2002-03-22 2007-06-26 Pharmacia & Upjohn Company Processes to prepare eplerenone
TW200409746A (en) * 2002-07-26 2004-06-16 Theravance Inc Crystalline β2 adrenergic receptor agonist
US20080081834A1 (en) 2002-07-31 2008-04-03 Lippa Arnold S Methods and compositions employing bicifadine for treating disability or functional impairment associated with acute pain, chronic pain, or neuropathic disorders
US7166641B2 (en) * 2002-10-02 2007-01-23 Yung Shin Pharmaceutical Industrial Co., Ltd. Pharmaceutically acceptable salts containing local anesthetic and anti-inflammatory activities and methods for preparing the same
RU2005117630A (ru) * 2002-11-08 2006-01-20 Дов Фармасьютикал, Инк. (Us) Полиморфы гидрохлорида бицифадина
TW200510277A (en) * 2003-05-27 2005-03-16 Theravance Inc Crystalline form of β2-adrenergic receptor agonist
US7384557B2 (en) * 2003-07-14 2008-06-10 Applied Ambient Extraction Process Consultants, Llc Method and apparatus for removing solute from a solid solute-bearing product
TWI328006B (en) 2003-12-26 2010-08-01 Nissan Chemical Ind Ltd Crystal form of quinoline compound and process for its production
US20070043100A1 (en) 2005-08-16 2007-02-22 Hagen Eric J Novel polymorphs of azabicyclohexane
US20060100263A1 (en) * 2004-11-05 2006-05-11 Anthony Basile Antipyretic compositions and methods
US20060100271A1 (en) * 2004-11-08 2006-05-11 Keith Whitehead Stabilized aqueous ranitidine compositions
AU2006275870B2 (en) 2005-07-27 2013-01-10 Otsuka America Pharmaceutical, Inc. Novel 1-aryl-3-azabicyclo[3.1.0]hexanes: preparation and use to treat neuropsychiatric disorders
DE102005035891A1 (de) * 2005-07-30 2007-02-08 Boehringer Ingelheim Pharma Gmbh & Co. Kg 8-(3-Amino-piperidin-1-yl)-xanthine, deren Herstellung und deren Verwendung als Arzneimittel
US20080045725A1 (en) * 2006-04-28 2008-02-21 Murry Jerry A Process For The Synthesis of (+) And (-)-1-(3,4-Dichlorophenyl)-3-Azabicyclo[3.1.0]Hexane
CA2756603C (en) * 2006-10-20 2013-05-28 Scinopharm Singapore Pte, Ltd. Process for making crystalline docetaxel trihydrate
US8138377B2 (en) 2006-11-07 2012-03-20 Dov Pharmaceutical, Inc. Arylbicyclo[3.1.0]hexylamines and methods and compositions for their preparation and use
EP2167083B1 (en) * 2007-06-06 2015-10-28 Euthymics Bioscience, Inc. 1- heteroaryl-3-azabicyclo[3.1.0]hexanes, methods for their preparation and their use as medicaments
US9133159B2 (en) 2007-06-06 2015-09-15 Neurovance, Inc. 1-heteroaryl-3-azabicyclo[3.1.0]hexanes, methods for their preparation and their use as medicaments
TW201011043A (en) * 2008-06-20 2010-03-16 Chugai Pharmaceutical Co Ltd Crystal of spiroketal derivatives and process for preparation of spiroketal derivatives
DK2727912T3 (da) 2011-06-30 2017-07-17 Toray Industries Krystaller af glycinderivat og farmaceutisk anvendelse deraf
US20140206740A1 (en) 2011-07-30 2014-07-24 Neurovance, Inc. Use Of (1R,5S)-(+)-(Napthalen-2-yl)-3-Azabicyclo[3.1.0]Hexane In The Treatment Of Conditions Affected By Monoamine Neurotransmitters
CN106432148B (zh) * 2015-05-26 2018-04-17 烟台市华文欣欣医药科技有限公司 一种治疗胃病的药物盐酸雷尼替丁化合物的制备方法
CN105030694A (zh) * 2015-08-04 2015-11-11 青岛蓝盛洋医药生物科技有限责任公司 一种治疗胃溃疡的药物盐酸雷尼替丁组合物干混悬剂
CN104971053A (zh) * 2015-08-05 2015-10-14 青岛蓝盛洋医药生物科技有限责任公司 一种治疗消化系统疾病的药物盐酸雷尼替丁组合物片剂
CN105055331A (zh) * 2015-08-31 2015-11-18 青岛蓝盛洋医药生物科技有限责任公司 一种治疗消化性溃疡的药物盐酸雷尼替丁组合物颗粒剂
WO2021079183A1 (en) * 2019-10-21 2021-04-29 Sms Pharmaceuticals Limited Isopropyl alcohol solvent free crystalline ranitidine hydrochloride form-2 which is free of nitrosamine (ndma) impurity

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GB1565966A (en) * 1976-08-04 1980-04-23 Allen & Hanburys Ltd Aminoalkyl furan derivatives
US4233302A (en) * 1977-12-23 1980-11-11 Glaxo Group Limited Amine derivatives and pharmaceutical compositions containing them

Also Published As

Publication number Publication date
SK403591A3 (en) 1995-08-09
AU7595581A (en) 1982-04-08
HK97985A (en) 1985-12-13
IE51604B1 (en) 1987-01-21
DK167794B1 (da) 1993-12-13
FR2491067B1 (da) 1984-09-07
ES505951A0 (es) 1983-01-01
DK436281A (da) 1982-04-02
IL63968A (en) 1985-10-31
DK167923B1 (da) 1994-01-03
AU549119B2 (en) 1986-01-16
MY8500747A (en) 1985-12-31
KR830007070A (ko) 1983-10-14
NZ198522A (en) 1985-07-12
SE8105812L (sv) 1982-04-02
DK33792A (da) 1992-03-12
ES8301954A1 (es) 1983-01-01
BE890574A (fr) 1982-04-01
IT8149407A0 (it) 1981-10-01
CH652122A5 (fr) 1985-10-31
KE3549A (en) 1985-08-16
JPS5791983A (en) 1982-06-08
CZ403591A3 (en) 1994-01-19
ZW24481A1 (en) 1983-04-27
PH19489A (en) 1986-05-14
LU83661A1 (fr) 1983-06-08
US4521431A (en) 1985-06-04
GR72499B (da) 1983-11-15
ZA816809B (en) 1983-05-25
CZ280885B6 (cs) 1996-04-17
DE3139134C2 (da) 1990-04-19
PH21761A (en) 1988-02-18
DE3139134A1 (de) 1982-05-19
NL8104482A (nl) 1982-05-03
AT389696B (de) 1990-01-10
IE812287L (en) 1982-04-01
JPH0443070B2 (da) 1992-07-15
IL63968A0 (en) 1981-12-31
IT1143237B (it) 1986-10-22
CA1202638A (en) 1986-04-01
ATA422281A (de) 1989-06-15
PT73744B (en) 1983-10-31
FR2491067A1 (fr) 1982-04-02
PT73744A (en) 1981-10-01
SK277922B6 (en) 1995-08-09
US4672133A (en) 1987-06-09
SE453500B (sv) 1988-02-08
KR870001431B1 (ko) 1987-08-06

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Legal Events

Date Code Title Description
B1 Patent granted (law 1993)
PUP Patent expired